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New Al III Zn II and Al III Cu II dinuclear complexes: Phosphatase-like activity and cytotoxicity.
- Source :
-
Journal of inorganic biochemistry [J Inorg Biochem] 2021 Jun; Vol. 219, pp. 111392. Date of Electronic Publication: 2021 Mar 13. - Publication Year :
- 2021
-
Abstract
- Herein, we report the synthesis and characterization of the first two Al <superscript>III</superscript> (μ-OH)M <superscript>II</superscript> (M = Zn (1) and Cu (2)) complexes with the unsymmetrical ligand H <subscript>2</subscript> L{2-[[(2-hydroxybenzyl)(2-pyridylmethyl)]aminomethyl]-6-bis(pyridylmethyl)aminomethyl}-4-methylphenol. The complexes were characterized through elemental analysis, X-ray crystallography, IR spectroscopy, mass spectrometry and potentiometric titration. In addition, complex 2 was characterized by electronic spectroscopy. Kinetics studies on the hydrolysis of the model substrate bis(2,4-dinitrophenyl)phosphate by 1 and 2 show Michaelis-Menten behavior, with 1 being slightly more active (8.31%) than 2 (at pH 7.0). The antimicrobial effect of the compounds was studied using four bacterial strains (Staphylococcus aureus, Pseudomonas aeuruginosa, Shigella sonnei and Shigella dysenteriae) and for both complexes the inhibition of bacterial growth was superior to that caused by sulfapyridine, but inferior to that of tetracycline. The dark cytotoxicity and photocytotoxicity (under UV-A light) of the complexes in a chronic myelogenous leukemia cell line were investigated. Complexes 1 and 2 exhibited significant cytotoxic activity against K562 cells, which undergoes a 2-fold increase on applying 5 min of irradiation with UV-A light. Complex 2 was more effective and a good correlation between cytotoxicity and intracellular concentration was observed, the intracellular copper concentration required to inhibit 50% of cell growth being 3.5 × 10 <superscript>-15</superscript>  mol cell <superscript>-1</superscript> .<br /> (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Subjects :
- Aluminum chemistry
Anti-Infective Agents pharmacology
Bacteria drug effects
Cell Survival drug effects
Coordination Complexes chemistry
Copper chemistry
Crystallography, X-Ray methods
Humans
Hydrolysis
K562 Cells
Kinetics
Ligands
Mass Spectrometry methods
Zinc chemistry
Aluminum pharmacology
Antineoplastic Agents pharmacology
Coordination Complexes pharmacology
Copper pharmacology
Phosphoric Monoester Hydrolases metabolism
Zinc pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3344
- Volume :
- 219
- Database :
- MEDLINE
- Journal :
- Journal of inorganic biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 33752123
- Full Text :
- https://doi.org/10.1016/j.jinorgbio.2021.111392